Molecular Modeling of Human P450c17 (17 -Hydroxylase/ 17,20-Lyase): Insights into Reaction Mechanisms and Effects of Mutations
Author:
Publisher
The Endocrine Society
Subject
Endocrinology,Molecular Biology,General Medicine
Cited by 183 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing;The Journal of Clinical Endocrinology & Metabolism;2024-06-27
2. Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients;Frontiers in Endocrinology;2022-12-15
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4. Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling;Pharmaceuticals;2021-10-01
5. Novel mutations of the CYP17A1 gene in four Chinese 46,XX cases with partial 17a-hydroxylase/17,20-lyase deficiency;Steroids;2021-09
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